十三烷二酸
| 十三烷二酸 | |
|---|---|
| |
| IUPAC名 tridecanedioic acid | |
| 识别 | |
| CAS号 | 505-52-2 
|
| PubChem | 10458 |
| 性质 | |
| 化学式 | C13H24O4 |
| 摩尔质量 | 244.33 g·mol−1 |
| 外观 | 白色固体 |
| 熔点 | 114 °C（387 K） |
| 溶解性（水） | 0.0025 g/100 mL |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
十三烷二酸（英语：tridecanedioic acid，别名巴西基酸，英语：Brassylic acid）是一种有机化合物，化学式为(CH
2)
11(CO
2H)
2。它可由芥酸（13-二十二烯酸）的催化氧化制得。[1]它具有羧酸的通性，如在硫酸存在下和甲醇发生酯化反应，得到十三烷二酸二甲酯；[2]和氯化亚砜回流反应，得到十三烷二酸二甲酰氯。[3]
参考文献
- ^ Renat Kadyrov, Dagmar Hackenberger. Oxidative Cleavage of Long Chain Olefins to Carboxylic Acids with Hydrogen Peroxide. Topics in Catalysis. 2014-11, 57 (17-20): 1366–1371 [2022-12-07]. ISSN 1022-5528. doi:10.1007/s11244-014-0304-6 （英语）.
- ^ Kenji Mori, Hiroyuki Nishio. Synthesis of sphingosine relatives, IX. Synthesis of (2S,3R,4E)-1-O-(β-D-glucopyranosyl)-N- [24-(linoleoyloxy)tetracosanoyl]-4-sphingenine. The structure proposed for the esterified cerebroside in the epidermis of guinea pigs. Liebigs Annalen der Chemie. 1991-03-12, 1991 (3): 253–257 [2022-12-07]. doi:10.1002/jlac.199119910143 （德语）.
- ^ Anna Zep, Kaja Sitkowska, Damian Pociecha, Ewa Gorecka. Photoresponsive helical nanofilaments of B 4 phase. J. Mater. Chem. C. 2014, 2 (13): 2323–2327 [2022-12-07]. ISSN 2050-7526. doi:10.1039/C3TC32325K （英语）.
| ||||||||||||||||||||||
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.
Cover photo is available under {{::mainImage.info.license.name || 'Unknown'}} license.
Cover photo is available under {{::mainImage.info.license.name || 'Unknown'}} license.
Credit:
(see original file).
